Carolinas ALS Center
Amyotrophic lateral sclerosis (ALS), commonly known as Lou
Gehrig's disease, is a progressive neurodegenerative disease that attacks motor
neurons in the brain (upper motor neurons) and spinal cord (lower motor
neurons).
These motor neurons control the movement of voluntary muscles. When the motor
neurons can no longer send impulses to the muscles due to ALS, the muscles begin
to waste away (atrophy), causing increased muscle weakness. Motor neuron, or
nerve cell, death makes it impossible for the brain to control muscles or signal
them to move.
Symptoms of ALS include twitching and cramping of muscles (called
fasciculation), loss of motor control in hands and arms, impaired use of the
arms and legs, weakness and fatigue, tripping and falling, dropping things,
slurred or thick speech and difficulty breathing or swallowing.
In most cases, ALS patients do not experience impaired intellectual reasoning,
vision or hearing. Eye and bladder muscles, along with sexual function and
drive, are not normally affected.
ALS is diagnosed using a variety of tests and examinations, including laboratory
tests, muscle and nerve biopsy, spinal tap, X-rays, MRI's and electrodiagnostic
tests.
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